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    1. Gill, P; Brenner, C; Brinkmann, B; Budowle, B; Carracedo, A; Jobling, MA; de Knijff, P; Kayser, M; Krawczak, M; Mayr, WR; Morling, N; Olaisen, B; Pascali, V; Prinz, M; Roewer, L; Schneider, PM; Sajantila, A; Tyler-Smith, C
      DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    2. Roewer, L; Krawczak, M; Willuweit, S; Nagy, M; Alves, C; Amorim, A; Anslinger, K; Augustin, C; Betz, A; Bosch, E; Caglia, A; Carracedo, A; Corach, D; Dekairelle, AF; Dobosz, T; Dupuy, BM; Furedi, S; Gehrig, C; Gusmao, L; Henke, J; Henke, L; Hidding, M; Hohoff, C; Hoste, B; Jobling, MA; Kargel, HJ; de Knijff, P; Lessig, R; Liebeherr, E; Lorente, M; Martinez-Jarreta, B; Nievas, P; Nowak, M; Parson, W; Pascali, VL; Penacino, G; Ploski, R; Rolf, B; Sala, A; Schmidt, U; Schmitt, C; Schneider, PM; Szibor, R; Teifel-Greding, J; Kayser, M
      Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypes

      FORENSIC SCIENCE INTERNATIONAL
    3. Krawczak, M
      Forensic evaluation of Y-STR haplotype matches: a comment

      FORENSIC SCIENCE INTERNATIONAL
    4. Lessig, R; Edelmann, J; Krawczak, M
      Population genetics of Y-chromosomal microsatellites in Baltic males

      FORENSIC SCIENCE INTERNATIONAL
    5. Krawczak, M; Boehringer, S; Epplen, JT
      Correcting for multiple testing in genetic association studies: the legendlives on

      HUMAN GENETICS
    6. Sauermann, U; Nurnberg, P; Bercovitch, FB; Berard, JD; Trefilov, A; Widdig, A; Kessler, M; Schmidtke, J; Krawczak, M
      Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaques

      HUMAN GENETICS
    7. Winter, H; Langbein, L; Krawczak, M; Cooper, DN; Jave-Suarez, LF; Rogers, MA; Praetzel, S; Heidt, PJ; Schweizer, J
      Human type I keratin pseudogene phi hHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence

      HUMAN GENETICS
    8. Al-Jader, LN; Harper, PS; Krawczak, M; Palmer, SR; Johansen, BN; Cooper, DN
      The frequency of inherited disorders database

      HUMAN GENETICS
    9. Hampe, J; Cuthbert, A; Croucher, PJP; Mirza, MM; Mascheretti, S; Fisher, S; Frenzel, H; King, K; Hasselmeyer, A; MacPherson, AJS; Bridger, S; van Deventer, S; Forbes, A; Nikolaus, S; Lennard-Jones, JE; Foelsch, UR; Krawczak, M; Lewis, C; Schreiber, S; Mathew, CG
      Association between insertion mutation in NOD2 gene and Crohn's disease inGerman and British populations

      LANCET
    10. Widdig, A; Nurnberg, P; Krawczak, M; Streich, WJ; Bercovitch, FB
      Paternal relatedness and age proximity regulate social relationships amongadult female rhesus macaques

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    11. Martin, MA; Rubio, JC; Garcia, A; Fernandez, MA; Campos, Y; Krawczak, M; Cooper, DN; Arenas, J
      Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease

      CLINICAL GENETICS
    12. Krawczak, M; Cooper, DN; Schmidtke, J
      Estimating the efficacy and efficiency of cascade genetic screening

      AMERICAN JOURNAL OF HUMAN GENETICS
    13. Kayser, M; Krawczak, M; Excoffier, L; Dieltjes, P; Corach, D; Pascali, V; Gehrig, C; Bernini, LF; Jespersen, J; Bakker, E; Roewer, L; de Knijff, P
      An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. Krawczak, M; Ball, EV; Fenton, I; Stenson, PD; Abeysinghe, S; Thomas, N; Cooper, DN
      Human gene mutation database - A biomedical information and research resource

      HUMAN MUTATION
    15. Cheadle, JP; Gill, H; Fleming, N; Maynard, J; Kerr, A; Leonard, H; Krawczak, M; Cooper, DN; Lynch, S; Thomas, N; Hughes, H; Hulten, M; Ravine, D; Sampson, JR; Clarke, A
      Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location

      HUMAN MOLECULAR GENETICS
    16. Morris, DW; Robinson, L; Turic, D; Duke, M; Webb, V; Milham, C; Hopkin, E; Pound, K; Fernando, S; Easton, M; Hamshere, M; Williams, N; McGuffin, P; Stevenson, J; Krawczak, M; Owen, MJ; O'Donovan, MC; Williams, J
      Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

      HUMAN MOLECULAR GENETICS
    17. Cheadle, JP; Gill, H; Fleming, N; Maynard, J; Kerr, A; Leonard, H; Krawczak, M; Cooper, DN; Lynch, S; Thomas, N; Hughes, H; Hulten, M; Ravine, D; Sampson, JR; Clarke, A
      Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location (vol 9, pg 1119, 2000)

      HUMAN MOLECULAR GENETICS
    18. Tischkowitz, M; Wheeler, D; France, E; Chapman, C; Lucassen, A; Sampson, J; Harper, P; Krawczak, M; Gray, J
      A comparison of methods currently used in clinical practice to estimate familial breast cancer risks

      ANNALS OF ONCOLOGY
    19. Roewer, L; Kayser, M; de Knijff, P; Anslinger, K; Betz, A; Caglia, A; Corach, D; Furedi, S; Henke, L; Hidding, M; Kargel, HJ; Lessig, R; Nagy, M; Pascali, VL; Parson, W; Rolf, B; Schmitt, C; Szibor, R; Teifel-Greding, J; Krawczak, M
      A new method for the evaluation of matches in non-recombining genomes: application to Y-chromosomal short tandem repeat (STR) haplotypes in European males

      FORENSIC SCIENCE INTERNATIONAL
    20. Chuzhanova, NA; Krawczak, M; Nemytikova, LA; Gusev, VD; Cooper, DN
      Promoter shuffling has occurred during the evolution of the vertebrate growth hormone gene

      GENE
    21. Millar, DS; Kemball-Cook, G; McVey, JH; Tuddenham, EGD; Mumford, AD; Attock, GB; Reverter, JC; Lanir, N; Parapia, LA; Reynaud, J; Meili, E; von Felton, A; Martinowitz, U; Prangnell, DR; Krawczak, M; Cooper, DN
      Molecular analysis of the genotype-phenotype relationship in factor VII deficiency

      HUMAN GENETICS
    22. Krawczak, M; Chuzhanova, NA; Stenson, PD; Johansen, BN; Ball, EV; Cooper, DN
      Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions

      HUMAN GENETICS
    23. Boehringer, S; Epplen, JT; Krawczak, M
      Genetic association studies of bronchial asthma - a need for Bonferroni correction?

      HUMAN GENETICS
    24. Millar, DS; Elliston, L; Deex, P; Krawczak, M; Wacey, AI; Reynaud, J; Nieuwenhuis, HK; Bolton-Maggs, P; Mannucci, PM; Reverter, JC; Cachia, P; Pasi, KJ; Layton, DM; Cooper, DN
      Molecular analysis of the genotype-phenotype relationship in factor X deficiency

      HUMAN GENETICS
    25. Antonarakis, SE; Krawczak, M; Cooper, DN
      Disease-causing mutations in the human genome

      EUROPEAN JOURNAL OF PEDIATRICS
    26. Dechend, F; Williams, G; Skawran, B; Schubert, S; Krawczak, M; Tyler-Smith, C; Schmidtke, J
      TSPY variants in six loci on the human Y chromosome

      CYTOGENETICS AND CELL GENETICS
    27. Schubert, S; Dechend, F; Skawran, B; Krawczak, M; Schmidtke, J
      Molecular evolution of the murine tspy genes

      CYTOGENETICS AND CELL GENETICS
    28. Hateboer, N; Veldhuisen, B; Peters, D; Breuning, MH; San-Millan, JL; Bogdanova, N; Coto, E; von Dijk, MA; Afzal, AR; Jeffery, S; Saggar-Malik, AK; Torra, R; Dimitrakov, D; Martinez, I; de Castro, SS; Krawczak, M; Ravine, D
      Location of mutations within the PKD2 gene influences clinical outcome

      KIDNEY INTERNATIONAL
    29. Sauermann, U; Stahl-Hennig, C; Stolte, N; Muhl, T; Krawczak, M; Spring, M; Fuchs, D; Kaup, FJ; Hunsmann, G; Sopper, S
      Homozygosity for a conserved Mhc class II DQ-DRB haplotype is associated with rapid disease progression in simian immunodeficiency virus-infected macaques: Results from a prospective study

      JOURNAL OF INFECTIOUS DISEASES
    30. Kayser, M; Roewer, L; Hedman, M; Henke, L; Henke, J; Brauer, S; Kruger, C; Krawczak, M; Nagy, M; Dobosz, T; Szibor, R; de Knijff, P; Stoneking, M; Sajantila, A
      Characteristics and frequency of germline mutations at microsatellite locifrom the human Y chromosome, as revealed by direct observation in father/son pairs

      AMERICAN JOURNAL OF HUMAN GENETICS
    31. Trefilov, A; Berard, J; Krawczak, M; Schmidtke, J
      Natal dispersal in rhesus macaques is related to serotonin transporter gene promoter variation

      BEHAVIOR GENETICS
    32. Hagelberg, E; Kayser, M; Nagy, M; Roewer, L; Zimdahl, H; Krawczak, M; Lio, P; Schiefenhovel, W
      Molecular genetic evidence for the human settlement of the Pacific: analysis of mitochondrial DNA, Y-chromosome and HLA markers

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    33. Krawczak, M; Chuzhanova, NA; Cooper, DN
      Evolution of the proximal promoter region of the mammalian growth hormone gene

      GENE
    34. Wacey, AI; Cooper, DN; Liney, D; Hovig, E; Krawczak, M
      Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53

      HUMAN GENETICS
    35. Krawczak, M
      Informativity assessment for biallelic single nucleotide polymorphisms

      ELECTROPHORESIS
    36. Trefilov, A; Krawczak, M; Berard, J; Schmidtke, J
      DNA sequence polymorphisms in genes involved in the regulation of dopamineand serotonin metabolism in rhesus macaques

      ELECTROPHORESIS
    37. Kehoe, P; Krawczak, M; Harper, PS; Owen, MJ; Jones, AL
      Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length

      JOURNAL OF MEDICAL GENETICS
    38. MILLAR DS; KRAWCZAK M; COOPER DN
      VARIATION OF SITE-SPECIFIC METHYLATION PATTERNS IN THE FACTOR-VIII (F8C) GENE IN HUMAN SPERM DNA

      Human genetics
    39. UPADHYAYA M; RUGGIERI M; MAYNARD J; OSBORN M; HARTOG C; MUDD S; PENTTINEN M; CORDEIRO I; PONDER M; PONDER BAJ; KRAWCZAK M; COOPER DN
      GROSS DELETIONS OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ARE PREDOMINANTLY OF MATERNAL ORIGIN AND COMMONLY ASSOCIATED WITH A LEARNING-DISABILITY, DYSMORPHIC FEATURES AND DEVELOPMENTAL DELAY

      Human genetics
    40. COOPER DN; BALL EV; KRAWCZAK M
      THE HUMAN GENE MUTATION DATABASE

      Nucleic acids research
    41. NURNBERG P; SAUERMANN U; KAYSER M; LANFER C; MANZ E; WIDDIG A; BERARD J; BERCOVITCH FB; KESSLER M; SCHMIDTKE J; KRAWCZAK M
      PATERNITY ASSESSMENT IN RHESUS MACAQUES (MACACA-MULATTA) - MULTILOCUSDNA-FINGERPRINTING AND PCR MARKER TYPING

      American journal of primatology
    42. KRAWCZAK M; COOPER DN
      P53 MUTATIONS, BENZO[A]PYRENE AND LUNG-CANCER

      Mutagenesis
    43. HUGHES HE; ALDERMAN JK; KRAWCZAK M; ROGERS C
      CONTRACTING FOR CLINICAL GENETIC SERVICES - THE WELSH MODEL

      Journal of Medical Genetics
    44. KRAWCZAK M; BALL EV; COOPER DN
      NEIGHBORING-NUCLEOTIDE EFFECTS ON THE RATES OF GERM-LINE SINGLE-BASE-PAIR SUBSTITUTION IN HUMAN GENES

      American journal of human genetics
    45. ROEWER L; KAYSER M; DIELTJES P; NAGY M; BAKKER E; KRAWCZAK M; DEKNIJFF P
      ANALYSIS OF MOLECULAR VARIANCE (AMOVA) OF Y-CHROMOSOME-SPECIFIC MICROSATELLITES IN 2 CLOSELY-RELATED HUMAN-POPULATIONS (VOL 5, PG 1029, 1996)

      Human molecular genetics
    46. JONES AC; DANIELLS CE; SNELL RG; TACHATAKI M; IDZIASZCZYK SA; KRAWCZAK M; SAMPSON JR; CHEADLE JP
      MOLECULAR-GENETIC AND PHENOTYPIC ANALYSIS REVEALS DIFFERENCES BETWEENTSC1 AND TSC2 ASSOCIATED FAMILIAL AND SPORADIC TUBEROUS SCLEROSIS

      Human molecular genetics
    47. KAYSER M; CAGLIA A; CORACH D; FRETWELL N; GEHRIG C; GRAZIOSI G; HEIDORN F; HERRMANN S; HERZOG B; HIDDING M; HONDA K; JOBLING M; KRAWCZAK M; LEIM K; MEUSER S; MEYER E; OESTERREICH W; PANDYA A; PARSON W; PENACINO G; PEREZLEZAUN A; PICCININI A; PRINZ M; SCHMITT C; SCHNEIDER PM; SZIBOR R; TEIFELGREDING J; WEICHOLD G; DEKNIJFF P; ROEWER L
      EVALUATION OF Y-CHROMOSOMAL STRS - A MULTICENTER STUDY

      International journal of legal medicine
    48. DEKNIJFF P; KAYSER M; CAGLIA A; CORACH D; FRETWELL N; GEHRIG C; GRAZIOSI G; HEIDORN F; HERRMANN S; HERZOG B; HIDDING M; HONDA K; JOBLING M; KRAWCZAK M; LEIM K; MEUSER S; MEYER E; OESTERREICH W; PANDYA A; PARSON W; PENACINO G; PEREZLEZAUN A; PICCININI A; PRINZ M; SCHMITT C; SCHNEIDER PM; SZIBOR R; TEIFELGREDING J; WEICHHOLD G; ROEWER L
      CHROMOSOME-Y MICROSATELLITES - POPULATION GENETIC AND EVOLUTIONARY ASPECTS

      International journal of legal medicine
    49. MACEK M; MACEK M; KREBSOVA A; NASH E; HAMOSH A; REIS A; VARONMATEEVA R; SCHMIDTKE J; MAESTRI NE; SPERLING K; KRAWCZAK M; CUTTING GR
      POSSIBLE ASSOCIATION OF THE ALLELE STATUS OF THE CS.7 HHAI POLYMORPHISM-5' OF THE CFTR GENE WITH POSTNATAL FEMALE SURVIVAL/

      Human genetics
    50. MAYNARD J; KRAWCZAK M; UPADHYAYA M
      CHARACTERIZATION AND SIGNIFICANCE OF 9 NOVEL MUTATIONS IN EXON-16 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE

      Human genetics
    51. WACEY AI; KRAWCZAK M; KEMBALLCOOK G; COOPER DN
      HOMOLOGY MODELING OF THE CATALYTIC DOMAIN OF EARLY MAMMALIAN PROTEIN-C - EVOLUTION OF STRUCTURAL FEATURES

      Human genetics
    52. SAUERMANN U; KRAWCZAK M; HUNSMANN G; STAHLHENNIG C
      IDENTIFICATION OF MHC-MAMU-DQB1 ALLELE COMBINATIONS ASSOCIATED WITH RAPID DISEASE PROGRESSION IN RHESUS MACAQUES INFECTED WITH SIMIAN IMMUNODEFICIENCY VIRUS

      AIDS
    53. KUHNAU W; BOHM I; KRAWCZAK M; SCHMIDTKE J
      A PATERNITY CASE WITH APPARENTLY CONFLICTING MULTILOCUS AND SINGLE-LOCUS DNA TYPING RESULTS

      Electrophoresis
    54. KAYSER M; DEKNIJFF P; DIELTJES P; KRAWCZAK M; NAGY M; ZERJAL T; PANDYA A; TYLERSMITH C; ROEWER L
      APPLICATIONS OF MICROSATELLITE-BASED Y-CHROMOSOME HAPLOTYPING

      Electrophoresis
    55. KRAWCZAK M; COOPER DN
      THE HUMAN-GENE-MUTATION-DATABASE

      Trends in genetics
    56. SCHMUCKER B; KRAWCZAK M
      MEIOTIC MICRODELETION BREAKPOINTS IN THE BRCA1 GENE ARE SIGNIFICANTLYASSOCIATED WITH SYMMETRICAL DNA-SEQUENCE ELEMENTS

      American journal of human genetics
    57. WIRTH B; SCHMIDT T; HAHNEN E; RUDNIKSCHONEBORN S; KRAWCZAK M; MULLERMYHSOK B; SCHONLING J; ZERRES K
      DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT OF INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE, AND IMPLICATIONS FOR GENETIC-COUNSELING

      American journal of human genetics
    58. UPADHYAYA M; MAYNARD J; RUGGIERI M; HUSON S; PONDER M; KRAWCZAK M; PONDER BAJ; COOPER DN
      A SEX BIAS IN THE ORIGIN OF NEW MUTATIONS IN THE NF1 GENE - THE NATURE OF MUTATIONS AND THEIR POSSIBLE MOLECULAR MECHANISMS

      American journal of human genetics
    59. WIRTH B; SCHMIDT T; HAHNEN E; RUDNIKSCHONEBORN S; KRAWCZAK M; MULLERMYHSOK B; SCHONLING J; ZERRES K
      DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE AND IMPLICATIONS FOR GENETIC-COUNSELING

      American journal of human genetics
    60. KRAWCZAK M; COOPER DN
      SINGLE BASE-PAIR SUBSTITUTIONS IN PATHOLOGY AND EVOLUTION - 2 SIDES TO THE SAME COIN

      Human mutation
    61. BADENS C; THURET I; MICHEL G; KRAWCZAK M; MATTEI JF; LENARUSSO D; LABIE D; ELION J
      NOVEL AND UNUSUAL DELETION-INSERTION THALASSEMIC MUTATION IN EXON-1 OF THE BETA-GLOBIN GENE

      Human mutation
    62. ROEWER L; KAYSER M; DIELTJES P; NAGY M; BAKKER E; KRAWCZAK M; DEKNIJFF P
      ANALYSIS OF MOLECULAR VARIANCE (AMOVA) OF Y-CHROMOSOME-SPECIFIC MICROSATELLITES IN 2 CLOSELY-RELATED HUMAN-POPULATIONS

      Human molecular genetics
    63. COOPER DN; KRAWCZAK M
      HUMAN GENE MUTATION DATABASE

      Human genetics
    64. KRAWCZAK M; WACEY A; COOPER DN
      MOLECULAR RECONSTRUCTION AND HOMOLOGY MODELING OF THE CATALYTIC DOMAIN OF THE COMMON ANCESTOR OF THE HEMOSTATIC VITAMIN-K-DEPENDENT SERINE PROTEINASES

      Human genetics
    65. PITRA C; CURSON A; NURNBERG P; KRAWCZAK M; BROWN S
      AN ASSESSMENT OF INBREEDING IN ASIAN WILD HORSE (EQUUS-PRZEWALSKII POLIAKOV 1881) POPULATIONS USING DNA-FINGERPRINTING

      Archiv fur Tierzucht
    66. KRAWCZAK M; SMITHSORENSEN B; SCHMIDTKE J; KAKKAR VV; COOPER DN; HOVIG E
      SOMATIC SPECTRUM OF CANCER-ASSOCIATED SINGLE BASEPAIR SUBSTITUTIONS IN THE TP53 GENE IS DETERMINED MAINLY BY ENDOGENOUS MECHANISMS OF MUTATION AND BY SELECTION

      Human mutation
    67. VARON R; MAGDORF K; STAAB D; WAHN HU; KRAWCZAK M; SPERLING K; REIS A
      RECURRENT NASAL POLYPS AS A MONOSYMPTOMATIC FORM OF CYSTIC-FIBROSIS ASSOCIATED WITH A NOVEL IN-FRAME DELETION (591DEL18) IN THE CFTR GENE

      Human molecular genetics
    68. WINTER PC; SCOPES DA; BERG LP; MILLAR DS; KAKKAR VV; MAYNE EE; KRAWCZAK M; COOPER DN
      FUNCTIONAL-ANALYSIS OF AN UNUSUAL LENGTH POLYMORPHISM IN THE HUMAN ANTITHROMBIN-III (AT3) GENE PROMOTER

      Blood coagulation & fibrinolysis
    69. SCOPES D; BERG LP; KRAWCZAK M; KAKKAR VV; COOPER DN
      POLYMORPHIC VARIATION IN THE HUMAN PROTEIN-C (PROC) GENE PROMOTER CANINFLUENCE TRANSCRIPTIONAL EFFICIENCY IN-VITRO

      Blood coagulation & fibrinolysis
    70. KRAWCZAK M
      LOCUS HOMOGENEITY FOR CARTILAGE-HAIR HYPOPLASIA PROVEN

      Human genetics
    71. KRAWCZAK M; REITSMA PH; COOPER DN
      THE MUTATIONAL DEMOGRAPHY OF PROTEIN-C DEFICIENCY

      Human genetics
    72. HALLAM PJ; WACEY AI; MANNUCCI PM; LEGNANI C; KUHNAU W; KRAWCZAK M; KAKKAR VV; COOPER DN
      A NOVEL MISSENSE MUTATION (THR176-]ILE) AT THE PUTATIVE HINGE OF THE NEO N-TERMINUS OF ACTIVATED PROTEIN-C

      Human genetics
    73. REITSMA PH; BERNARDI F; DOIG RG; GANDRILLE S; GREENGARD JS; IRELAND H; KRAWCZAK M; LIND B; LONG GL; POORT SR; SAITO H; SALA N; WITT I; COOPER DN
      PROTEIN-C DEFICIENCY - A DATABASE OF MUTATIONS, 1995 UPDATE

      Thrombosis and haemostasis
    74. KRAWCZAK M; LUBJUHN T
      AN INFORMATIVITY INDEX FOR MULTILOCUS DNA FINGERPRINTS

      Electrophoresis
    75. KRAWCZAK M; COOPER DN
      CORE DATABASE

      Nature
    76. STUHRMANN M; KRAWCZAK M; SCHMIDTKE J
      POTENTIALS AND LIMITS OF THE MOLECULAR DI AGNOSIS OF CYSTIC-FIBROSIS

      Monatsschrift fur Kinderheilkunde
    77. HALLAM PJ; MILLAR DS; KRAWCZAK M; KAKKAR VV; COOPER DN
      POPULATION DIFFERENCES IN THE FREQUENCY OF THE FACTOR-V LEIDEN VARIANT AMONG PEOPLE WITH CLINICALLY SYMPTOMATIC PROTEIN-C DEFICIENCY

      Journal of Medical Genetics
    78. DORK T; WILL K; GRADE K; KRAWCZAK M; TUMMLER B
      A 32-BP DELETION (2991DEL32) IN THE CYSTIC-FIBROSIS GENE ASSOCIATED WITH CFTR MESSENGER-RNA REDUCTION

      Human mutation
    79. BARTELS I; BOCKEL B; CAESAR J; KRAWCZAK M; THIELE M; RAUSKOLB R
      RISK OF FETAL DOWNS-SYNDROME BASED ON MATERNAL AGE AND VARYING COMBINATIONS OF MATERNAL SERUM MARKERS

      Archives of gynecology and obstetrics
    80. MERTES G; LUDWIG M; FINKELNBURG B; KRAWCZAK M; SCHWAAB R; BRACKMANN HH; OLEK K
      A G(-TO-T DONOR SPLICE-SITE MUTATION LEADS TO SKIPPING OF EXON-50 IN VON-WILLEBRAND-FACTOR MESSENGER-RNA(3))

      Genomics
    81. WACEY AI; KRAWCZAK M; KAKKAR VV; COOPER DN
      DETERMINANTS OF THE FACTOR-IX MUTATIONAL SPECTRUM IN HEMOPHILIA-B - AN ANALYSIS OF MISSENSE MUTATIONS USING A MULTIDOMAIN MOLECULAR-MODEL OF THE ACTIVATED

      Human genetics
    82. KRAWCZAK M
      MULTILOCUS DNA-FINGERPRINTING - THE INDEPENDENCE PROBLEM IN QUANTITATIVE PATERNITY TESTING

      Electrophoresis
    83. KRAWCZAK M; SCHMIDTKE J; EPPLEN JT; HANSMANN I; THIES U
      A MULTILOCUS DNA FINGERPRINT WITH BUILT-IN SECURITY DEVICES

      Medicine, Science and the Law
    84. KRAWCZAK M; BOHM I; NURNBERG P; HAMPE J; HUNDRIESER J; POCHE H; PETERS C; SLOMSKI R; KWIATKOWSKA J; NAGY M; POPPER A; EPPLEN JT; SCHMIDTKE J
      PATERNITY TESTING WITH OLIGONUCLEOTIDE MULTILOCUS PROBE (CAC)5 (GTG)5- A MULTICENTER STUDY/

      Forensic science international
    85. MILLAR DS; KRAWCZAK M; TUDDENHAM EGD; KAKKAR VV; COOPER DN
      LOCALIZATION OF ALU AND LINE REPETITIVE SEQUENCES IN THE HUMAN FACTOR-VIII (F8) GENE - RELATIONSHIP TO GENE DELETIONS CAUSING HEMOPHILIA-A

      Thrombosis and haemostasis
    86. KRAWCZAK M; BERARD JD; BERCOVITCH FB; SCHMIDTKE J; NURNBERG P
      POWER AND LIMITS OF DNA-PROFILING IN PRIMATE POPULATIONS - PATERNITY ASSESSMENT IN RHESUS MACAQUES FROM CAYO-SANTIAGO

      Primates


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Documento generato il 04/12/20 alle ore 19:39:21